HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-benzyl-4-methoxycarbonyl-4-(N-phenylmethoxyacetamido)piperidine → 4-methoxycarbonyl-4-(N-phenylmethoxyacetamido)piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-benzyl-4-methoxycarbonyl-4-(N-phenylmethoxyacetamido)piperidine | HCID 23324838 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 4-methoxycarbonyl-4-(N-phenylmethoxyacetamido)piperidine | HCID 23324821 | — |
Reaction Steps
A mixture of 12.45 g of 1-benzyl-4-methoxycarbonyl-4-(N-phenylmethoxyacetamido)piperidine and 250 ml of acetic acid is hydrogenated at room temperature and pressure with 1.5 g of 10% palladium-on-charcoal catalyst. After the calculated amount of hydrogen is taken up, the catalyst is filtered off. The acetic acid is flash evaporated, the residue is dissolved in toulene and stirred with 10 g of anhydrous sodium carbonate. The solid is filtered and the filtrate is flash evaporated to obtain 4-methoxycarbonyl-4-(N-phenylmethoxyacetamido)piperidine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04584303 |
| Source dataset | uspto-grants-1986_04 |
| ORD ID | ord-cbccb428274b419395cd1469a0960944 |
| Source note | uspto-grants-1986_04 |